TCTR20200805001已完成2 期
Effectiveness of Traditional Thai massage on muscle stiffness in patients with myofascial pain syndrome
Research Administration Division (KKU)0 个研究点开始时间: 2020年8月5日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20 Years 至 60 Years（—）
- 性别
- All
入选标准
- •1. Male or female between 20 to 50 years old
- •2. Performed within office work four or more hours a day, and suffered from neck or shoulder pain corresponding with the upper trapezius muscle.
- •3. Experiencing spontaneous shoulder pain (VAS more than 3) longer than 12 weeks (chronic) and at least one trigger point in the upper trapezius
- •muscle. Trigger points diagnosed as the presence of local tenderness within a taut band and with pain recognition.
- •4. CROM limited in direction of lateral neck flexion to the opposite side of a TrP within upper trapezius muscle.
- •5. Able to follow instructions
- •6. Good communication and cooperation
排除标准
- •1. A history of the following diseases or disorders:
- •1.1 The abnormality of muscle structure Other diseases at
- •cervicothoracic shoulder
- •1.2 Post-surgical at cervicothoracic shoulder
- •1.3 Bone fracture or joint dislocation
- •1.4 Severed osteoporosis
- •1.5 Hemophilia
- •2. Contraindications of traditional Thai massage
- •2.1 Contagious skin disease
- •2.2 Injury or inflammation of muscle
- •2.3 Open wound
- •2.4 Alcohol intoxication
- •3. Hypertension, diabetes, heart disease
- •4. Received medication, e.g., warfarin, enoxaparin,heparin.
- •5. BMI more than 30
- •Withdrawal criteria
- •1. Muscle pain during receives the treatment
- •2. Receives another massage during join our research
- •3. The participant wants to leave all cases
- •MRI and MRE
- •1. The researcher has to checked before used in the
- •1.1 Metallic joint prostheses
- •1.2 Artificial heart valves
- •1.3 Implantable heart defibrillator
- •1.4 Pacemaker
- •1.5 Metal clips
- •1.6 Cochlear implants
- •1.7 Bullet, shrapnel or any other type of metal
- •2. Absolute contraindication to perform MRI and MRE
- •2.1 Aneurysm clip(s), any metallic fragment or foreign body, coronary
- •and peripheral artery stents, aortic stent graft, prosthetic
- •heart valves, and annuloplasty rings, cardiac occluder devices,
- •vena cava filters, and embolization coils
- •2.2 Hemodynamic monitoring and temporary
- •pacing devices, e.g., hemodynamic support devices, cardiac pacemaker, implanted cardioverter-defibrillator (ICD), retained transvenous pacemaker and defibrillator leads
- •2.3 Electronic implant or device, e.g., insulin pump or other infusion pumps
- •2.4 Permanent contraceptive devices,
- •diaphragm, or pessary
- •2.5 Cochlear, otologic, or other ear implants
- •2.6 Neurostimulation system
- •2.7 Shunt (spinal or intraventricular)
- •2.8 Vascular access port or catheter
- •2.9 A tissue expander (e.g., breast)
- •2.10 Joint replacement (e.g., hip, knee, and other)
- •2.11 Hearing aid
- •2.12 Any type of prosthesis (e.g., eye, penile, and
- •2.13 Tattoo or permanent makeup
- •3. The participants who have any symptoms, e.g., Known
- •claustrophobia, known/ possible pregnancy or breastfeeding, pregnancy or lactation, advanced stage of cancer, and sepsis, infected the influenza virus (H5N1, H7N7, and H9N2 subtypes unable to lay still in the supine position, and unstable vital signs
- •Withdrawal criteria: MRI and MRE
- 另有 4 项未显示
研究者
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